Colon Cancer: Gene >> SIX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648706:60648706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>A
AA Mutation	p.Gly162Ser(p.G162S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60649092:60649092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98T>C
AA Mutation	p.Phe33Ser(p.F33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648999:60648999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191G>A
AA Mutation	p.Arg64His(p.R64H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648846:60648846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>G
AA Mutation	p.Phe115Cys(p.F115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60646363:60646363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Gly259Ser(p.G259S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648636:60648636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554A>C
AA Mutation	p.Lys185Thr(p.K185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60649009:60649009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>A
AA Mutation	p.Gly61Ser(p.G61S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60646535:60646535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603C>A
AA Mutation	p.Asn201Lys(p.N201K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247182
Start	60649124:60649124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247182
Start	60649067:60649067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247182
Start	60646388:60646388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247182
Start	60648761:60648761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648786:60648786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404C>T
AA Mutation	p.Ser135Leu(p.S135L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247182
Start	60648651:60648651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript